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dc.contributor.advisorNaser, Iftekhar Bin
dc.contributor.advisorRakib-Uz-Zaman, S M
dc.contributor.authorNASIFUZZAMAN, S M
dc.date.accessioned2021-12-12T05:50:14Z
dc.date.available2021-12-12T05:50:14Z
dc.date.copyright2021
dc.date.issued2021-08
dc.identifier.otherID 17336015
dc.identifier.urihttp://hdl.handle.net/10361/15720
dc.descriptionThis thesis is submitted in partial fulfillment of the requirements for the degree of Bachelor of Science in Biotechnology 2021.en_US
dc.descriptionCatalogued from PDF version of thesis.
dc.descriptionIncludes bibliographical references (pages 42-47).
dc.description.abstractEvery year during the rainy season in Bangladesh severe Dengue infection is widespread throughout the country. Aedes aegypti and Ae. Albopictus are the two vectors that are responsible for the transmission of the virus. Thousands of lives including infants, adults, and old people die and many suffer painful fever due to this infection. In some severe cases, the patients experience a drastic decrease in their platelet count which sometimes causes hemorrhage and eventually leads to death. To protect lives against the Dengue virus, vaccination is an effective method. In our study, we have designed a vaccine against the Dengue virus by reverse vaccinology method. We have developed our vaccine targeting the envelope protein since it is highly conserved and immunogenic. Our study was mainly focused on predicting the right B cell epitopes, Cytotoxic T cell epitopes, and Helper T cell epitopes. These epitopes will be the key component of the vaccine. Stimulation of these cells in the body will help to acquire both Humoral and Cell-mediated immunity. As our study followed a immunoinformatics approach we employed various online bioinformatics tools and servers for epitope prediction.en_US
dc.description.statementofresponsibilityS M NASIFUZZMAN
dc.format.extent47 pages
dc.language.isoenen_US
dc.publisherBrac Universityen_US
dc.rightsBrac University theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission.
dc.subjectEnvelope proteinen_US
dc.subjectReverse vaccinologyen_US
dc.subjectMulti-epitope vaccineen_US
dc.subjectB cellen_US
dc.subjectCTLen_US
dc.subjectHTLen_US
dc.subjectImmunoinformatics approachen_US
dc.subject.lcshDengue viruses
dc.titleDeveloping a novel multi-epitope vaccine against Dengue virus targeting the Envelope protein using an Immunoinformatics approachen_US
dc.typeThesisen_US
dc.contributor.departmentDepartment of Mathematics and Natural Sciences, Brac University
dc.description.degreeB. Biotechnology


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